Showing 481 - 490 of 515 annotations tagged with the keyword "Disability"
A middle aged woman goes backpacking for the first time in 14 years after losing her leg in an automobile accident. As she recounts the excursion, with its difficulties and exhilaration, she reflects on the ways her life was changed by losing her leg, and the emotional journey she has taken since the accident. She concludes by thinking about how to find power despite her vulnerability, how to adjust and accommodate, but never compromise.
A woman, Rose, describes her childhood during the depression as she struggled with issues of her own identity and her jealousy toward her younger sister, Sophie, who suffers from cerebral palsy and seizures. Rose watches as Sophie is born, as her parents argue, as Sophie is held closely by their mother during her seizures, and as Sophie is given two birthday parties each year. She fantasizes about how life might be if her sister were dead, and imagines her sister hanging from a rack like the animals at the slaughterhouse. Finally, she discovers that Sophie actually needs her and loves her.
Summary:In this collection, sixteen writers (including the editor, in her introduction) recount the deaths of one or both of their parents. They explore a wide range of questions: about the relationship between parents and their children, about the inevitability of the loss of that relationship (if it is lost in death, for, as the editor asks, "is the death of a parent really the end of the relationship?" [p. 2]), and about the conflicts that arise between the necessary separation that comes with adulthood and the complex ongoing attachments which in these stories enrich, haunt, inform and in many ways determine the lives of the tellers.
This is the second of 13 short autobiographical pieces in the book, Naked. In it, Sedaris describes, in vivid and humorous detail, the obsessive compulsive behavior that plagued his life from grade school into college. From licking every light switch encountered, to counting each of "six hundred and thirty-seven steps" on the way home from school, "pausing every few feet to tongue a mailbox" and having to retrace his steps if he lost count, Sedaris was compelled to " . . . do these things because nothing was worse than the anguish of not doing them."
Each year, a teacher called on his mother to discuss the strange tics. His mother took his behavior and these visits in stride: "The kid's wound too tight, but he'll come out of it. So, what do you say, another scotch, Katherine?" "She suggested my teachers interpret my jerking head as a nod of agreement. 'That's what I do, and now I've got him washing the dishes for the next five years.'"
Life became more complicated when Sedaris entered college and had to contend with a roommate. There are amusing descriptions of the elaborate stratagems that he devised to conceal or explain the tics. Finally, "my nervous habits faded about the same time I took up with cigarettes . . . more socially acceptable than crying out in tiny voices."
This book is a series of essays about the illness experience. The author developed chronic fatigue syndrome (CFS) after a viral illness in 1988. Suddenly, this 41-year-old public policy analyst, who was also a successful writer and a competitive runner, was thrust into the world of severe disability. He developed subtle but extensive neurological deficits that affected his concentration and memory. For months he could hardly get out of bed. He discovered that not only was the cause of CFS unknown, many physicians did not even believe it was a "real" illness.
"Double Blind" tells the story of Skloot's participation in an ill-fated clinical trial of Ampligen, an experimental treatment for CFS. Other essays describe the author's experience with alternative medicine, including an intensive course of Ayurvedic "detoxification" ("Healing Powers") and a visit to Germany to encounter Mother Meera, an avatar of the Divine Mother ("Honeymooning With the Feminine Divine").
"Home Remedies" presents his comic experience with helpful calls and letters telling him how to get rid of the illness. Other essays deal with Skloot's learning to cope with chronic disability. A final section includes poems about the illness experience of several composers and artists (e.g. Carl Maria von Weber, George Gershwin, and Vincent van Gogh).
Summary:The Giant's House is narrated by Peggy Cort, a young librarian in a small Cape Cod town in the early 1950s. She falls in love--and her life becomes inextricably tangled--with James Sweatt, a young boy who suffers from gigantism.
In Book I Oliver Sacks describes his visit to Pingelap and Pohnpei in the Caroline Islands (now a part of the Federated States of Micronesia). On Pingelap (population 700) 5-10% of the people are completely colorblind; i.e. they have a rare hereditary condition called achromatopsia in which the retina has no functional cone cells. Rod cells, which normally provide peripheral and night vision, are their only source of vision. While partial colorblindness is common, achromatopsia is normally very rare. Sacks and Knut Nordby, a Norwegian scientist who is himself achromatopic, examined dozens of achromatopes on Pingelap and in a village of Pingelapese people on the larger Pohnpei.
In Book II Sacks takes the reader to Guam where he investigates (with his friend John Steele, a neurologist who lives on the island) the neurological disease called "lytico-bodig." The "lytico" form of this disease is a progressive paralysis similar to amyotropic lateral sclerosis, while the "bodig" form resembles parkinsonism. Both appeared in Guam after the Second World Way and now seem to be dying out. However, no one has ever determined their cause.
Sacks tells the story of his visit, while also discussing various hypotheses that have been considered and discarded over forty years of study. The last section of the book describes a trip to Rota, a small island north of Guam, where Sacks visits a forest of cycad trees and discusses his life-long fascination with these primitive plants.
Summary:The poem, written in German, appears in both German and English in this and other versions. Those who understand German may feel that something has been lost in translation, inevitable for rhyming poetry. Nevertheless the "endless outcry" of isolation and bitterness is well expressed. This blind man is totally unresigned to his condition; "every day I despair." He feels himself uniquely cursed. He mocks those who are sighted for believing that THEY might be special and he is contemptuous of any kindness shown him: no one can understand how he feels.
Summary:The poet has "grown quite good at ignoring" the suffering people who beg in the streets of India. "The beautiful legless girl," "the spider man," the babies with swollen bellies--he has learned to be almost blind to the poverty, disease and deformity that surrounds him. Or, at least, he pretends not to see, and then tries to sneak a photograph. He knows that if he tried to help these people, "next time / they would claw me to shreds."
The memoir is divided into roughly two halves: before Mike's death and after Mike's death. The narrator is one of the dying man's circle of gay and lesbian friends, and becomes, for unclear reason's, his most involved caregiver. She goes to his apartment on summons at any hour, flies to Memphis when Michael is hospitalized after collapsing, loans him money, and endures relentless psychological abuse as his cognitive powers fade.
In the second half of the book, the writer reflects. Her anger toward Mike's disease, AIDS, and Mike himself does not seem tempered by the passage of time. She is still struggling at the end of the tale, more than two years after Mike's death.